| Product NDC: | 0519-1452 |
| Proprietary Name: | Kindest Kare Antimicrobial Foaming Handwash |
| Non Proprietary Name: | Triclosan |
| Active Ingredient(s): | .75 g/100mL & nbsp; Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0519-1452 |
| Labeler Name: | STERIS Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20060314 |
| Package NDC: | 0519-1452-41 |
| Package Description: | 1000 mL in 1 BOTTLE (0519-1452-41) |
| NDC Code | 0519-1452-41 |
| Proprietary Name | Kindest Kare Antimicrobial Foaming Handwash |
| Package Description | 1000 mL in 1 BOTTLE (0519-1452-41) |
| Product NDC | 0519-1452 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclosan |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20060314 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | STERIS Corporation |
| Substance Name | TRICLOSAN |
| Strength Number | .75 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |